nsv515478
- Organism: Homo sapiens
- Study:nstd55 (Zhu et al. 2011)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:7,917
- Publication(s):Zhu et al. 2011
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 607 SVs from 51 studies. See in: genome view
Overlapping variant regions from other studies: 607 SVs from 51 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv515478 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000023.11 | ChrX | 140,412,870 | 140,420,786 |
| nsv515478 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000023.10 | ChrX | 139,495,035 | 139,502,951 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis |
|---|---|---|---|---|
| nssv650714 | deletion | 4 | Sequencing | Sequence alignment |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| nssv650714 | Remapped | Perfect | NC_000023.11:g.140 412870_140420786de l | GRCh38.p12 | First Pass | NC_000023.11 | ChrX | 140,412,870 | 140,420,786 |
| nssv650714 | Submitted genomic | NC_000023.10:g.139 495035_139502951de l | GRCh37 (hg19) | NC_000023.10 | ChrX | 139,495,035 | 139,502,951 |